Seizure outcome trajectories in a well‐defined cohort of newly diagnosed juvenile myoclonic epilepsy patients.

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Title: Seizure outcome trajectories in a well‐defined cohort of newly diagnosed juvenile myoclonic epilepsy patients.
Authors: Cerulli Irelli, Emanuele (AUTHOR), Morano, Alessandra (AUTHOR), Orlando, Biagio (AUTHOR), Salamone, Enrico M. (AUTHOR), Fanella, Martina (AUTHOR), Fattouch, Jinane (AUTHOR), Manfredi, Mario (AUTHOR), Giallonardo, Anna T. (AUTHOR), Di Bonaventura, Carlo (AUTHOR)
Source: Acta Neurologica Scandinavica. Mar2022, Vol. 145 Issue 3, p314-321. 8p.
Subjects: Myoclonus, Epilepsy, People with epilepsy, Seizures (Medicine), Logistic regression analysis, Prognosis, Diagnosis
Abstract: Objective: To investigate the temporal course of medication response and associated prognostic factors in a cohort of juvenile myoclonic epilepsy (JME) patients over a long‐term follow‐up. Materials and Methods: Data from 113 JME patients diagnosed according to recently proposed class II criteria were retrospectively reviewed. Early sustained remission was defined as 4‐year seizure remission starting within 2 years from the first antiseizure medication (ASM) intake, as opposed to delayed sustained remission. Spontaneous relapse rate (ie, not related to ASM withdrawal) was also investigated, along with factors associated with seizure relapse. Results: Four‐year seizure remission was obtained by 76/113 (67.3%) subjects. Early sustained remission was achieved by 45/76 (59.2%) patients. Absence seizures were significantly associated with no‐remission at multivariable multinomial logistic regression analysis. Catamenial seizures and earlier age at epilepsy onset significantly predicted delayed sustained remission. Spontaneous seizure relapse after 4‐year remission occurred in 15.7% of patients with early sustained remission and in 35.5% of those with delayed sustained remission (p = 0.045). The most common concomitant factors for a spontaneous relapse were irregular lifestyle habits and pregnancy‐related switch from valproate to another ASM. Patients with a history of catamenial seizures were more likely to experience a spontaneous generalized tonic‐clonic seizure relapse after 4‐year remission at univariable analysis. Significance: Our data support the prognostic relevance of early medication response in JME patients. Furthermore, the prognostic significance of catamenial seizures and the impact of valproate switch on seizure relapse after a prolonged remission account for the challenging therapeutic management of women with childbearing potential. [ABSTRACT FROM AUTHOR]
Copyright of Acta Neurologica Scandinavica is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Seizure outcome trajectories in a well‐defined cohort of newly diagnosed juvenile myoclonic epilepsy patients.
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  Data: <searchLink fieldCode="AR" term="%22Cerulli+Irelli%2C+Emanuele%22">Cerulli Irelli, Emanuele</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Morano%2C+Alessandra%22">Morano, Alessandra</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Orlando%2C+Biagio%22">Orlando, Biagio</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Salamone%2C+Enrico+M%2E%22">Salamone, Enrico M.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fanella%2C+Martina%22">Fanella, Martina</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fattouch%2C+Jinane%22">Fattouch, Jinane</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Manfredi%2C+Mario%22">Manfredi, Mario</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Giallonardo%2C+Anna+T%2E%22">Giallonardo, Anna T.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Di+Bonaventura%2C+Carlo%22">Di Bonaventura, Carlo</searchLink> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Acta+Neurologica+Scandinavica%22">Acta Neurologica Scandinavica</searchLink>. Mar2022, Vol. 145 Issue 3, p314-321. 8p.
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  Data: <searchLink fieldCode="DE" term="%22Myoclonus%22">Myoclonus</searchLink><br /><searchLink fieldCode="DE" term="%22Epilepsy%22">Epilepsy</searchLink><br /><searchLink fieldCode="DE" term="%22People+with+epilepsy%22">People with epilepsy</searchLink><br /><searchLink fieldCode="DE" term="%22Seizures+%28Medicine%29%22">Seizures (Medicine)</searchLink><br /><searchLink fieldCode="DE" term="%22Logistic+regression+analysis%22">Logistic regression analysis</searchLink><br /><searchLink fieldCode="DE" term="%22Prognosis%22">Prognosis</searchLink><br /><searchLink fieldCode="DE" term="%22Diagnosis%22">Diagnosis</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: Objective: To investigate the temporal course of medication response and associated prognostic factors in a cohort of juvenile myoclonic epilepsy (JME) patients over a long‐term follow‐up. Materials and Methods: Data from 113 JME patients diagnosed according to recently proposed class II criteria were retrospectively reviewed. Early sustained remission was defined as 4‐year seizure remission starting within 2 years from the first antiseizure medication (ASM) intake, as opposed to delayed sustained remission. Spontaneous relapse rate (ie, not related to ASM withdrawal) was also investigated, along with factors associated with seizure relapse. Results: Four‐year seizure remission was obtained by 76/113 (67.3%) subjects. Early sustained remission was achieved by 45/76 (59.2%) patients. Absence seizures were significantly associated with no‐remission at multivariable multinomial logistic regression analysis. Catamenial seizures and earlier age at epilepsy onset significantly predicted delayed sustained remission. Spontaneous seizure relapse after 4‐year remission occurred in 15.7% of patients with early sustained remission and in 35.5% of those with delayed sustained remission (p = 0.045). The most common concomitant factors for a spontaneous relapse were irregular lifestyle habits and pregnancy‐related switch from valproate to another ASM. Patients with a history of catamenial seizures were more likely to experience a spontaneous generalized tonic‐clonic seizure relapse after 4‐year remission at univariable analysis. Significance: Our data support the prognostic relevance of early medication response in JME patients. Furthermore, the prognostic significance of catamenial seizures and the impact of valproate switch on seizure relapse after a prolonged remission account for the challenging therapeutic management of women with childbearing potential. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of Acta Neurologica Scandinavica is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.1111/ane.13556
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      – Code: eng
        Text: English
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        PageCount: 8
        StartPage: 314
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      – SubjectFull: Myoclonus
        Type: general
      – SubjectFull: Epilepsy
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      – SubjectFull: People with epilepsy
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      – SubjectFull: Seizures (Medicine)
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      – SubjectFull: Logistic regression analysis
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      – SubjectFull: Prognosis
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      – SubjectFull: Diagnosis
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      – TitleFull: Seizure outcome trajectories in a well‐defined cohort of newly diagnosed juvenile myoclonic epilepsy patients.
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              Text: Mar2022
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              Y: 2022
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